Crouzon Syndrome

Below you will find more information about Crouzon Syndrome from Medigest. If you believe that you are suffering from any of the symptoms of Crouzon Syndrome it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Crouzon Syndrome and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Crouzon Syndrome comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.

Definition

The hereditary disorder Crouzon syndrome arises when the bones of a baby's skull and face close early or are incapable of expanding. This abnormal bone development is caused by disturbances in the development of the branchial arches and leads to malformation of the skull and facial features. Typically, individuals with Crouzon syndrome have low-lying ears and malformed ear canals that cause hearing loss.

Diagnosis

To diagnose the disease, doctors need radiographs, genetic testing and magnetic resonance imaging (MRI).

Treatment

Surgery is necessary to prevent the premature fusion of sutures from doing damage to a patient's brain's development. When the closure goes unchecked, Crouzon syndrome may result to mental incapacity and blindness. Surgery is also advisable to correct the malformations in the patient's features.

Symptoms and Signs

Because of their pronounced features, infants afflicted with Crouzon syndrome are diagnosed with the disease early. The manifestations of the disorder include short and wide head, bulging eyes, beak-like nose, concave-shaped face, and hypertelorism (distance between eyes is bigger than normal. Patients may also encounter problems with their nose, teeth, sinuses, and palate.

Causes

Crouzon syndrome results from disturbances in the development of branchial arches, maxilla and mandible. It affects one in every 25,000 persons. It is not hereditary.

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